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Class II · ModerateActive recall

Metoclopramide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign Tablets/Capsules

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byTeva Pharmaceuticals USA, Inc.
Brand nameMETOCLOPRAMIDE
Generic nameMETOCLOPRAMIDE
Active ingredient(s)METOCLOPRAMIDE HYDROCHLORIDE
Distributed by / forTeva Pharmaceuticals, Parsippany, NJ 07054
Show the full FDA record
Full product labelMetoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05
Recalling firmTeva Pharmaceuticals USA, Inc
DistributionUS Nationwide.
Quantity240,448 cartons
Recall initiated2026-09-29
Report date2026-10-21
Recall completed—
Recall numberD-0038-2027
ClassificationClass II
FDA statusOngoing
Origin on fileParsippany NJ United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.